Virtual Reality on Perception of Pain and Anxiety by Hysteroscopy (Hysteroscopy)

Intervention Study to Measure the Effect on Perception of Pain and Anxiety in Women With Indication for Diagnostic Hysteroscopy Through the Use of Virtual Reality

Randomized intervention trial with a calculated sample size of 90 women aged between 18 and 75 years and medical criteria for performing a diagnostic hysteroscopy according to the Gynecology and Obstetrics Spanish Society (SEGO).

Nowadays the investigators known that acute pain requires cognitive attention for its perception, a patient's state of anxiety depends on the subjective capacity to cope with the process and that environments created with virtual reality can cause a cognitive distraction that diminishes the perception of pain as well as a subjective psychological illusion that diminishes the anxiety that motivates the procedure.

For all the above, the investigators will study as a main objective the differences between the use of virtual reality through the use of virtual reality glasses "Oculus go model", to reduce the perception of pain and anxiety motivated by the performance of a outpatient hysteroscopy versus clinical practice. It is usual not to use analgesia, using the VAS pain scale and the STAI (State-Trait Anxiety Inventory) questionnaire to assess the state of anxiety before and after the test. In addition, as secondary objectives, the investigators will compare different aspects such as surgical time used, determination of vital signs, satisfaction studies ...

Study Overview

• Status: Terminated
• Conditions: Uterine Diseases
• Intervention / Treatment: Device: Hysteroscopy & virtual reality glasses; Device: Hysteroscopy

Detailed Description

A Cochrane review (included 32 clinical trials and 3304 patients) concluded that there was no effective and safe treatment for pain relief in patients undergoing outpatient hysteroscopy. In the same way, The Gynecology and Obstetrics Spanish Society (SEGO) discourages the routine use of analgesics prior to the test or the use of local anesthesia or sedation, since neither improves the pain nor the satisfaction of the patients in this type of test.

Nowadays, is knowed that acute pain requires cognitive attention for its perception, a patient's state of anxiety depends on the subjective capacity to cope with the process and that environments created with virtual reality can cause a cognitive distraction that diminishes the perception of pain as well as a subjective psychological illusion that diminishes the anxiety that motivates the procedure.

With all this, the investigators intend to assess through this study if patients with medical indication for diagnostic hysteroscopy can benefit from the use of Virtual Reality for the decrease in their perception of pain, anxiety or increase in the degree of satisfaction with their performance.

1. - Design: Randomized intervention clinical trial
2. - Sample: by contrast of hypothesis, a sample size of 90 women with an established medical indication for outpatient hysteroscopy was determined. They were randomized using excel software. As criteria of inclusion, those of SEGO with ages between 18 and 75 years were used. Criteria of exclusion those of the test, presenting some type of illness or disability that contraindicate the use of Virtual Reality (blindness, deafness, epilepsy, etc), voluntary wish of no inclusion or inability to understand the study.

3. - Methodology:

   • parameters to analyze:

     • the average decrease in the perception of pain in both groups using the Visual Analogue Scale (VAS) with determinations at the end, at 15 and 30 minutes.
     • the average decrease in the perception of the state of anxiety using the State-Trait Anxiety Inventory (STAI) questionnaire prior to the performance of the test and after it.
     • Modifications in the degree of satisfaction with the test by means of a STAI questionnaire included in the protocol of the Gynecology Service of El Escorial University Hospital.
     • Changes in parameters such as blood pressure, heart rate and oxygen saturation before, during and after hysteroscopy.
     • The influence of different circumstances such as age, parity, on the painful perception, state of anxiety or degree of satisfaction in both arms of the study.
   • A 5 mm Bettocchi hysteroscope model will be used as a physiological serum distension medium and initial irrigation pressures of 75 mm Hg.
   • Semi-rigid 5 Charr instruments (scissors, grasping forceps and biopsy).
   • Oculus Go virtual reality glasses.
   • The recruitment time will be that necessary to obtain the sample size.
   • The patients will be given the STAI anxiety scale that will be completed prior to accessing the room. Once sitting on the examination table, a pulse oximeter will be placed on the left index finger, a cuff for measuring blood pressure on the right arm, and in the selected group virtual reality glasses, the first determination of blood pressure, heart rate and oxygen saturation is made at this time and will be repeated when accessing the endometrial cavity and immediately after removing the hysteroscope. After completing the test, still sitting and removed the virtual reality components will be given VAS for pain determination during the test. After dressing, the pain will be assessed using VAS at 15 and 30 minutes after the end of the test. Before leaving, a new STAI anxiety state will be delivered that will complete as well as respond to the two questions of the satisfaction protocol.

• Study Type: Interventional
• Enrollment (Actual): 154
• Phase: Not Applicable

Contacts and Locations

• Study Contact: Name: David V Varillas Delgado, PhD; Phone Number: +34 617068714; Email: david.varillas@ufv.es
• Study Contact Backup: Name: Jesús V Pelazas Hernández, MD; Phone Number: +34 630945535; Email: jesuspelazas@hotmail.com

Study Locations

• Spain
  • Madrid
    • Pozuelo de Alarcón, Madrid, Spain, 28224
      • David Varillas Delgado

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: 18 years to 75 years (Adult, Older Adult)
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Women with an established indication for diagnostic hysteroscopy according to the Spanish Society of Gynecology and Obstetrics (SEGO) criteria collected in its document of consensus, updated in 2013, with the title of "Hysteroscopy in consultation".
• Age between 18 and 75 years.
• Suitable cultural level for the understanding of the characteristics of the study.
• Signature of informed consent.

Exclusion Criteria:

• Not be within the criteria established by SEGO for the realization of a hysteroscopy diagnostic.
• Existence of contraindication for hysteroscopy.
• Present some type of disease or disability that can intervene in the object of the study: visual deficit, auditory or sensory severe, illnesses or mental syndromes.
• Having suffered seizures, loss of knowledge, or other symptoms related to epileptic disorders that discourages the use of virtual reality glasses.
• Women who cannot tolerate the pain at the beginning and during hysteroscopy.
• Not signature of informed consent.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Prevention
• Allocation: Randomized
• Interventional Model: Parallel Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Hysteroscopy & Virtual reality glasses; Hysteroscopy with use of virtual reality glasses	Device: Hysteroscopy & virtual reality glasses; Hysteroscopy. Virtual reality glasses. VAS. STAI scale.; Device: Hysteroscopy; Hysteroscopy. VAS. STAI scale.
Active Comparator: Hysteroscopy; Hysteroscopy without use of virtual reality glasses	Device: Hysteroscopy; Hysteroscopy. VAS. STAI scale.

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Visual Analogue Scale (VAS)	Visual Analogue Scale: A measurement instrument that tries to measure a characteristic or attitude that is believed to range across a continuum of values and cannot easily be directly measured.This scale is between the values 0 to 10, being 0 the greatest pain possible and 10 the least pain. It is categorized into several sections, being intense pain 0-3, moderate pain 4-7 and low pain 8-10.	Change from baseline VAS at 30 minutes.
State-Trait Anxiety Inventory (STAI)	State-Trait Anxiety Inventory (STAI): A psychological inventory based on a 4-point Likert scale and consists of 40 questions on a self-report basis. The STAI measures two types of anxiety - state anxiety, or anxiety about an event, and trait anxiety, or anxiety level as a personal characteristic. Scores range from 20 to 80, with higher scores correlating with greater anxiety. Each measure has a different rating scale. The 4-point scale for S-anxiety is as follows: 1.) not at all, 2.) somewhat, 3.) moderately so, 4.) very much so. The 4-point scale for T-anxiety is as follows: 1.) almost never, 2.) sometimes, 3.) often, 4.) almost always.	Change from baseline STAI scale at 30 minutes.

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Systolic and Diastolic blood pressure	Analize both blood pressures (systolic and diastolic) modifications in patients of study, experimental and active comparator groups.	Changes of systolic and diastolic blood pressure from baseline at 30 minutes.
Cardiac frequency	Analize cardiac frenquence modifications in intervention group previous procedure, during the procedure and at the end of procedure.	Changes of cardiac frequency from baseline at 30 minutes.
Oxygen saturation	Analize oxygen saturation modifications in intervention group previous procedure, during the procedure and at the end of procedure.	Changes of oxygen saturation from baseline at 30 minutes.

Collaborators and Investigators

• Sponsor: Universidad Francisco de Vitoria
• Collaborators: Jesús Pelazas Hernández; David Varillas Delgado; Ignacio Cristóbal García; Teresa González Casado; Ignacio Cristóbal Quevedo; Agustina Alonso Bermejo; Marina Ronchas Martínez
• Investigators: Principal Investigator: Jesús V Pelazas Hernández, MD, Hospital El Escorial

Study record dates

Study Major Dates

• Study Start (Actual): March 30, 2019
• Primary Completion (Actual): October 30, 2019
• Study Completion (Actual): December 31, 2020

Study Registration Dates

• First Submitted: January 24, 2019
• First Submitted That Met QC Criteria: January 30, 2019
• First Posted (Actual): February 1, 2019

Study Record Updates

• Last Update Posted (Actual): May 19, 2023
• Last Update Submitted That Met QC Criteria: May 17, 2023
• Last Verified: July 1, 2022

More Information

Terms related to this study

• Keywords: Pain; Anxiety; Virtual Reality; Hysteroscopy
• Additional Relevant MeSH Terms: Uterine Diseases
• Other Study ID Numbers: 12.18

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: UNDECIDED

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No